Recent development of monoamine oxidase inhibitors

被引:35
作者
Bolasco, A [1 ]
Fioravanti, R [1 ]
Carradori, S [1 ]
机构
[1] Univ Roma La Sapienza, Dipartimento Studi Chim & Tecnol Sostanze Biol At, I-00185 Rome, Italy
关键词
N-acylamminoaryl derivative; Alzheimer's disease; amido propargylamine; anxiety; cinnamide; dementia; depression; diterpene; fluorobenzamide; imidazole; isoindole; isoquinoline; oxazole; Parkinson's disease; phenanthrene; phthalimide; pyridine; pyrrolidine; thiazole;
D O I
10.1517/13543776.15.12.1763
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The monoamine oxidases (MAO-A and MAO-B) are flavoenzymes located in the outer mitochondrial membrane responsible for the oxidative deamination of many endogenous and exogenous monoamines. Recognition of the importance of monoamine oxidases as targets for drug intervention for the treatment of a variety of conditions, such as schizophrenia, Alzheimer's disease, Parkinson's disease and other psychiatric and neurological disorders, has produced an enormous interest in the development of molecules that act as inhibitors on these enzymes. This review mainly focuses on the numerous monoamine oxidase inhibitor (MAO-I)-related patents published from August 2002 to June 2005. In this paper recent developments of monoamine oxidase inhibitors are reported, ordering all patents by molecular structure. A structure-activity relationship (SAR) study that reports on known MAO inhibitors is also outlined before a discussion on new associations with other drugs of classical MAO inhibitors and their new target.
引用
收藏
页码:1763 / 1782
页数:20
相关论文
共 81 条
[11]  
CESURA AM, 1990, MOL PHARMACOL, V37, P358
[12]   METABOLISM OF THE NEUROTOXIC TERTIARY AMINE, MPTP, BY BRAIN MONOAMINE-OXIDASE [J].
CHIBA, K ;
TREVOR, A ;
CASTAGNOLI, N .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1984, 120 (02) :574-578
[13]   PHARMACOLOGY OF A NEW PHTHALANE (LU 10-171), WITH SPECIFIC 5-HT UPTAKE INHIBITING PROPERTIES [J].
CHRISTENSEN, AV ;
FJALLAND, B ;
PEDERSEN, V ;
DANNESKIOLDSAMSOE, P ;
SVENDSEN, O .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1977, 41 (02) :153-162
[14]   Three-dimensional structure of human monoamine oxidase A (MAO A): Relation to the structures of rat MAO A and human MAO B [J].
De Colibus, L ;
Li, M ;
Binda, C ;
Lustig, A ;
Edmondson, DE ;
Mattevi, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (36) :12684-12689
[15]   Pro-apoptotic gene expression mediated by the p38 mitogen-activated protein kinase signal transduction pathway [J].
De Zutter, GS ;
Davis, RJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (11) :6168-6173
[16]  
DELASSAUNIERE C, 2005, Patent No. 38087
[17]   The FAD binding sites of human monoamine oxidases A and B [J].
Edmondson, DE ;
Binda, C ;
Mattevi, A .
NEUROTOXICOLOGY, 2004, 25 (1-2) :63-72
[18]  
ELI LILLY CO, 2002, Patent No. 02050067
[19]   TYRAMINE ANTAGONISTIC PROPERTIES OF AGN-1135, AN IRREVERSIBLE INHIBITOR OF MONOAMINE-OXIDASE TYPE-B [J].
FINBERG, JPM ;
TENNE, M ;
YOUDIM, MBH .
BRITISH JOURNAL OF PHARMACOLOGY, 1981, 73 (01) :65-74
[20]   THE ACETYLENIC MONOAMINE-OXIDASE INHIBITORS CLORGYLINE, DEPRENYL, PARGYLINE AND J-508 - THEIR PROPERTIES AND APPLICATIONS [J].
FOWLER, CJ ;
ORELAND, L ;
CALLINGHAM, BA .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1981, 33 (06) :341-347